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Markers of JC virus infection in patients with multiple sclerosis under natalizumab therapy
OBJECTIVE: To evaluate the frequency of JC polyomavirus (JCPyV) infection and anti-JCPyV antibodies in patients with multiple sclerosis under natalizumab therapy. METHODS: Presence of anti-JCPyV antibodies and JCPyV DNA was analyzed in 39 patients with relapsing-remitting multiple sclerosis undergoi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299884/ https://www.ncbi.nlm.nih.gov/pubmed/25610882 http://dx.doi.org/10.1212/NXI.0000000000000058 |
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author | Clausi, Valeria Giannecchini, Simone Magnani, Eliana Repice, Anna Mechi, Claudia Martelli, Francesco Azzi, Alberta Massacesi, Luca |
author_facet | Clausi, Valeria Giannecchini, Simone Magnani, Eliana Repice, Anna Mechi, Claudia Martelli, Francesco Azzi, Alberta Massacesi, Luca |
author_sort | Clausi, Valeria |
collection | PubMed |
description | OBJECTIVE: To evaluate the frequency of JC polyomavirus (JCPyV) infection and anti-JCPyV antibodies in patients with multiple sclerosis under natalizumab therapy. METHODS: Presence of anti-JCPyV antibodies and JCPyV DNA was analyzed in 39 patients with relapsing-remitting multiple sclerosis undergoing natalizumab therapy. Anti-JCPyV antibodies were evaluated in serum by a 2-step virus-like particle-based ELISA assay (Stratify), and JCPyV DNA was evaluated in peripheral blood mononuclear cells, plasma, and urine by quantitative PCR. The anti-JCPyV antibodies were evaluated in serum samples collected at the same time or later than those collected for DNA analysis. RESULTS: JCPyV DNA was detected in 59% of patients, and anti-JCPyV antibodies were present in 67%. JCPyV DNA occurred more often in blood than in urine. Anti-JCPyV antibodies were observed in 70% of the JCPyV-infected patients, and JCPyV DNA was detected in 50% of the patients without anti-JCPyV antibodies. When JCPyV DNA was investigated in blood and urine the frequency of infection was higher than previously described. CONCLUSION: Under these experimental conditions, with respect to the observed frequency of JCPyV infection, the sensitivity of the anti-JCPyV antibody assay was lower than expected. |
format | Online Article Text |
id | pubmed-4299884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-42998842015-01-21 Markers of JC virus infection in patients with multiple sclerosis under natalizumab therapy Clausi, Valeria Giannecchini, Simone Magnani, Eliana Repice, Anna Mechi, Claudia Martelli, Francesco Azzi, Alberta Massacesi, Luca Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: To evaluate the frequency of JC polyomavirus (JCPyV) infection and anti-JCPyV antibodies in patients with multiple sclerosis under natalizumab therapy. METHODS: Presence of anti-JCPyV antibodies and JCPyV DNA was analyzed in 39 patients with relapsing-remitting multiple sclerosis undergoing natalizumab therapy. Anti-JCPyV antibodies were evaluated in serum by a 2-step virus-like particle-based ELISA assay (Stratify), and JCPyV DNA was evaluated in peripheral blood mononuclear cells, plasma, and urine by quantitative PCR. The anti-JCPyV antibodies were evaluated in serum samples collected at the same time or later than those collected for DNA analysis. RESULTS: JCPyV DNA was detected in 59% of patients, and anti-JCPyV antibodies were present in 67%. JCPyV DNA occurred more often in blood than in urine. Anti-JCPyV antibodies were observed in 70% of the JCPyV-infected patients, and JCPyV DNA was detected in 50% of the patients without anti-JCPyV antibodies. When JCPyV DNA was investigated in blood and urine the frequency of infection was higher than previously described. CONCLUSION: Under these experimental conditions, with respect to the observed frequency of JCPyV infection, the sensitivity of the anti-JCPyV antibody assay was lower than expected. Lippincott Williams & Wilkins 2015-01-14 /pmc/articles/PMC4299884/ /pubmed/25610882 http://dx.doi.org/10.1212/NXI.0000000000000058 Text en © 2015 American Academy of Neurology This is an open access article distributed under the terms of the Creative Commons Attribution-Noncommercial No Derivative 3.0 License, which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially. |
spellingShingle | Article Clausi, Valeria Giannecchini, Simone Magnani, Eliana Repice, Anna Mechi, Claudia Martelli, Francesco Azzi, Alberta Massacesi, Luca Markers of JC virus infection in patients with multiple sclerosis under natalizumab therapy |
title | Markers of JC virus infection in patients with multiple sclerosis under natalizumab therapy |
title_full | Markers of JC virus infection in patients with multiple sclerosis under natalizumab therapy |
title_fullStr | Markers of JC virus infection in patients with multiple sclerosis under natalizumab therapy |
title_full_unstemmed | Markers of JC virus infection in patients with multiple sclerosis under natalizumab therapy |
title_short | Markers of JC virus infection in patients with multiple sclerosis under natalizumab therapy |
title_sort | markers of jc virus infection in patients with multiple sclerosis under natalizumab therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299884/ https://www.ncbi.nlm.nih.gov/pubmed/25610882 http://dx.doi.org/10.1212/NXI.0000000000000058 |
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